Quality Control Analyst I, Raw Materials

Role: QC Analyst I, Raw Materials at a biopharma company specializing in innovative ophthalmic therapies, responsible for routine and non-routine testing of raw materials to ensure compliance with industry and regulatory standards. Responsibilities: perform qualitative and quantitative analyses using techniques such as HPLC, GC, FTIR, and UV-Vis; review and interpret analytical data; support raw material qualification, requalification, and external testing coordination; assist in document preparation including SOPs, test protocols, and reports; investigate out-of-specification results; participate in audits and ensure lab safety. Requirements: Bachelor’s in Chemistry, Biochemistry, or related field; 1–3 years laboratory experience in a regulated environment; proficiency in analytical techniques; understanding of cGMP, GLP, and regulatory guidelines; strong documentation and organizational skills; ability to work independently and collaboratively. Preferred: experience with LIMS, familiarity with compendial testing (USP, EP, JP), knowledge of raw material lifecycle management. High-Value: role in supporting compliance and quality assurance for raw materials in ophthalmic drug development and manufacturing. Work Environment: laboratory setting with chemical exposure; may involve lifting up to 25 lbs; PPE required.